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FDA 510(k)

INQU PASTE MIX PLUS

K-Number: K103799 · 2011-08-29

ApplicantIsto Technologies, Inc.
Decision Date2011-08-29
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INQU PASTE MIX PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Isto Technologies, Inc.. It received FDA 510(k) clearance on 2011-08-29 under 510(k) number K103799. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INQU PASTE MIX PLUS?

INQU PASTE MIX PLUS is a medical device that received FDA 510(k) clearance on 2011-08-29. The listed applicant is Isto Technologies, Inc.. The 510(k) number is K103799.

When did INQU PASTE MIX PLUS receive FDA 510(k) clearance?

INQU PASTE MIX PLUS received FDA 510(k) clearance on 2011-08-29, under 510(k) number K103799.

Who is the listed applicant for INQU PASTE MIX PLUS?

The FDA 510(k) record lists Isto Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INQU PASTE MIX PLUS?

The FDA product code for INQU PASTE MIX PLUS is MQV.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Isto Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K111838INQU PASTE MIXK071428INQUK063359INQU

Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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